Genomics Solutions Tailored for You

DNA Sequencing

  • Genomic (WGS - High-Depth & Low-Pass)

  • Amplicon (eDNA, Whole Metabiome)

  • Barcoded (MGI or Illumina)

  • Bisulphite

  • ChiP-seq

  • Hi-C

RNA Sequencing

  • Whole Transcriptome

  • PolyA 3’ sequencing

  • rRNA Depletion (Human, Mouse, Plant, Fungus)

  • Poly-A Enrichment

MGI-Specific Workflows

  • Spatial Transcriptomics (STOmics)

    STOmics on any species using fresh frozen or FFPE-Paraffin embedded samples

  • Synthetic Long Fragment Read (stLFR)

    stLFR technology achieves high accuracy (>Q30) reads at N50’s >40Kb

Our sequencing technology provides over 90% of reads with Q40 accuracy (99.99%), requiring fewer reads for high-confidence base calling, with flexible throughput options.

Same industry-standard FASTQ, but with higher accuracy and volume.

We offer library synthesis services with the ability to sequence any short-read library after conversion. Our services include:

Choose from two flow cell sizes and various sequencing options to suit your project.

FCS (2 Lanes)

FCL (4 Lanes)

Sequencing Lengths:

Pair-end:

  • PE50

  • PE100

  • PE150

  • PE300

Single-end:

  • SE50

  • SE100

  • SE150

  • SE300

We guarantee 400 million features per lane (800 million pair-end reads), with data volumes in-excess of this passed onto you free of charge

Sample Preparation Service

Lincoln Genomics can extract your RNA, DNA and also PCR 16S, 18S and ITS for metabarcoding. 

 For a quote please enter your sequencing project requirements here: Quotation form

 Or contact customer support at: ngs@lincoln.ac.nz or call: (+64) 3 423 0924

We are happy to help with new sequencing technologies

Schedule your complimentary genomics consultation today